drugset / Trial / NCT03546621

A Multicenter, Open-label, Randomized Clinical Study to Assess Efficacy and Safety of 3 Doses of Myrcludex B for 24 Weeks in Combination With Tenofovir Compared to Tenofovir Alone to Suppress HBV Replication in Patients With Chronic Hepatitis D

NCT03546621

Phase 2 Completed 120 enrolled Hepatera Ltd. Data Matrix Solutions · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multicenter, open-label, randomized clinical trial to Assess Efficacy and Safety of 3 Doses of Myrcludex B for 24 Weeks in Combination with Tenofovir Compared to Tenofovir Alone to Suppress HBV Replication in Patients with Chronic Hepatitis D

Timeline

Start
2016-02-16
Primary completion
2018-01-31
Completion
2018-01-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Myrcludex B Peptide 2 mg Subcutaneous
Subject Myrcludex B Peptide 5 mg Subcutaneous
Subject Myrcludex B Peptide 10 mg Subcutaneous
Subject Tenofovir Small molecule 245 mg Oral